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STERRAD™

ADVANCED STERILIZATION PRODUCTS SERVICES INC. · Model 20229 · UDI-DI 10705037016501

2
510(k) clearances
0
Adverse events
0
Recalls
0
Facilities

Description

STERRAD™ 100NX Validation Kit

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.